510(k) K172042 ยท GZL Electrode, Depth
NeuroNav System, NeuroSmart System
| Applicant | Alpha Omega Engineering , Ltd., Nazareth, IL |
| Decision | Substantially Equivalent, Feb 27, 2018 |
| Received | Jul 6, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172042
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.